8-Chloro-1,7-naphthyridine is a heterocyclic organic compound characterized by a fused bicyclic structure containing nitrogen atoms. It features a chlorine substituent at the 8-position of the naphthyridine ring system, which contributes to its chemical reactivity and potential biological activity. This compound is typically a pale yellow to light brown solid, exhibiting moderate solubility in organic solvents. Its molecular structure allows for various interactions, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the chlorine atom can influence its electronic properties and reactivity, potentially enhancing its ability to interact with biological targets. Additionally, 8-chloro-1,7-naphthyridine may exhibit properties such as antimicrobial or anti-inflammatory activity, although specific biological effects would depend on further studies. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile compound in synthetic organic chemistry.

8-chloro-1,7-naphthyridine

13058-77-0: 8-Chloro-1,7-naphthyridine is a heterocyclic organic compound characterized by a fused bicyclic structure containing nitrogen atoms. It features a chlorine substituent at the 8-position of the naphthyridine ring system, which contributes to its chemical reactivity and potential biological activity. This compound is typically a pale yellow to light brown solid, exhibiting moderate solubility in organic solvents. Its molecular structure allows for various interactions, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the chlorine atom can influence its electronic properties and reactivity, potentially enhancing its ability to interact with biological targets. Additionally, 8-chloro-1,7-naphthyridine may exhibit properties such as antimicrobial or anti-inflammatory activity, although specific biological effects would depend on further studies. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, making it a versatile compound in synthetic organic chemistry.

CAS 13058-77-0

8-chloro-1,7-naphthyridine

1,7-Naphthyridine, 8-chloro-

Ref: IN-DA000UOW

8-Chloro-1,7-naphthyridine

Ref: 54-OR300334

8-Chloro-1,7-naphthyridine

Ref: 10-F233274